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Chromosomal Aberrations and Sister Chromatid Exchanges in Lymphocytes and Urine Mutagenicity of Migraine Patients: A Comparison of Chronic Feverfew Users and Matched Non-users

Genetic and Reproductive Toxicology and Cell Biology Department, BIBRA, Woodmansterne Road, Carshalton Surrey SM5 4DS

P.C. Jenkinson

Genetic and Reproductive Toxicology and Cell Biology Department, BIBRA, Woodmansterne Road, Carshalton Surrey SM5 4DS

R.S. Dewdney

Genetic and Reproductive Toxicology and Cell Biology Department, BIBRA, Woodmansterne Road, Carshalton Surrey SM5 4DS

S.D. Blowers

Genetic and Reproductive Toxicology and Cell Biology Department, BIBRA, Woodmansterne Road, Carshalton Surrey SM5 4DS

E.S. Johnson

The City of London Migraine Clinic, 22 Charterhouse Square, London EC1M 6DX, UK

N.P. Kadam

The City of London Migraine Clinic, 22 Charterhouse Square, London EC1M 6DX, UK

1 Thirty migraine patients who had taken the leaves, tablets or capsules of feverfew daily for more than 11 consecutive months were compared to 30 feverfew non-user migraine patients who had been individually age- and sex-matched.

2 The frequency of chromosomal aberrations and sister chromatid exchanges (SCE) were determined from lymphocyte cultures established from blood samples taken over a period of several months. Matched pairs were sampled on the same date for two-thirds of the cases, and the greatest difference in sampling time of the remainder was 20 days. Also, the mutagenicity of urine samples from 10 feverfew user migraine patients was compared to that from 10 matched non-user migraine patients using the Ames Salmonella mutagenicity test system. Paired samples were given on the same date.

3 The mean frequency of chromosomal aberrations in the feverfew user group was lower than that in the non-user group both in terms of cells with breaks (2.13% vs 2.76%) and in terms of cells with all aberrations (4.34% vs 5.11%). However, this difference was small and not significant.

4 The mean frequency of SCE in the feverfew exposed group was lower than that in the control group (8.78 vs 8.80 SCE/cell), but, this difference was not significant as determined by factorial analysis of variance (P = 0.897). There was a highly significant variance between the frequencies of SCE in the matched pairs of migraine patients but this was not related to age, sex or feverfew exposure.

5 The mean number of revertants in the Ames mutagenicity assay was greater for the urine of the feverfew user migraine patients than that of the non-user migraine patients, in both strains of bacteria, with or without the inclusion of an S-9 metabolizing system. However, the increases were small and not significant.

6 The data indicate that the prophylactic use of feverfew for the alleviation of migraine symptoms affects neither the frequency of chromosomal aberrations nor the frequency of SCE in the circulating peripheral lymphocytes. Also, the mutagenicity of urine from feverfew user migraine patients is unaffected compared to urine from non-user migraine patients detectable by the methods used in this study.

Human & Experimental Toxicology, Vol. 7, No. 2, 145-152 (1988)
DOI: 10.1177/096032718800700207


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